Spectroscopic Insight into Tetrahedrally Distorted Square Planar Copper(II) Complex: XRD/HSA, Physicochemical, DFT, and Thermal Investigations

The reaction of bidentate N-S-thione-Schiff base, (E)-benzyl 2-(1-(4-chlorophenyl)-ethylidene)hydrazinecarbodithioate, with Cu(NO3)2·3H2O produced a cis-Cu(II) complex. The molecular structure was confirmed and characterized by CHN-EA, FAB-MS, IR, and UV-Vis analyses. The XRD supported cis-isomer of the bis anionic bidentate N (azomethine) and S (thiol) ligand coordination mode in tetrahedrally distorted square planar, rarely reported in the literature. The results of the XRD-bond lengths were in perfect agreement with the density functional theory (DFT) calculation. DFT-calculated angles around the Cu(II) center displayed slightly less distortion around the metal center from those of XRD. Additionally, the thermal stability of the complex was evaluated via thermal gravimetric analysis (TGA). Two-dimensional fingerprint (2D-FP), Hirshfeld surface analysis (HSA), and molecular electrostatic potential (MEP) support the XRD-packing results with the existence of the H⸱⸱⸱Cl and CH⸱⸱⸱π bonds as the main interactions in the crystal lattice of the desired complex.


Introduction
Recently, a wide spectrum of nitrogen-and sulfur-including ligands like dithiocarbazates, thiosemicarbazones, and dithiocarbamates with their metal ion complexes have experienced supplementary interest in the field of medicine and pharmacology due to their potent applications, such as antibacterial, antiviral, antitumor, antifungal, and antiparasitic activities [1][2][3][4][5][6][7][8]. The structural variation on hydrazinecarbodithioate Schiff base derivatives, R-CH=N-NH-C(=S)-S-NHR, can be easily modified through the replacement of R groups in the synthetic steps. Therefore, a broad selection of N,N or N,S and N,N,S or N,N,N as bidentate, tridentate, and even polydentate ligands has been prepared for medicinal and industrial application as well as for evaluating the coordination modes with transition metals [9][10][11][12][13][14][15][16][17][18][19][20]. The hydrazinecarbodithioate Schiff bases derived from S-acetyl, S-alkyl, S-methyl dithiocarbazates, and dithiocarbazate represent the preponderance of advanced reports available on the Cambridge Structural Database. However, only a limited number are accessible on hydrazinecarbodithioate with substituted S-benzyl moiety along with their organometallic complexes [8][9][10][11][12][13][14]. Despite the fact that coordinated hydrazinecarbodithioate Schiff bases to transition metals are scarcely reported and demonstrated on compared to the free ligands, full characterization by XRD analysis is highly demanded in order to obtain a real structural vision.
The spatial arrangement of four coordinated groups around the metal center offers several geometries, mostly regular tetrahedral, occasionally square planar, and rarely tetrahedrally distorted square planar, resulting in either increasing the bond angles (elongated tetrahedron) or decreasing the angles (flattened tetrahedron) [21][22][23]. Furthermore, a square planar molecular geometry could be created once the four groups are located at the corners of a square in the same plane of the central metal, with the possibility of possessing cis or trans conformation, e.g., M(N,S) 2 , in which N,S is a bidentate ligand. Quite rarely, a hybrid molecular geometry, namely, a tetrahedrally distorted square planar shape, can be formed due to the distorted coordinated ligand moieties to the metal center [22,23]. Thus, structural elucidation by XRD analysis offers an excellent level of characterization of the geometry around metal complexes.
Herein, we depict the synthesis of tetrahedrally distorted square planar complexes, rising from the in situ tautomerization of hydrazine-1-carbodithioate derivative and subsequent coordination with Cu(NO 3 ) 2 ·3H 2 O after deprotonating the thiol group in the absence of base. The new Cu(II) complex was fully described by XRD, revealing a cis conformation of the two coordinated ligands to the metal ion. Furthermore, the thermal behavior, physicochemical properties, Hirshfeld surface analysis (HSA), and density functional theory (DFT) simulations were investigated and demonstrated.

Computational
HSA was executed using the CrystalExplorer software, version 17 (version 17, University of Western Australia, Perth, Australia) [24]. Gaussian W09 Revision E.01 software [25] was employed for all DFT operations. Optimization and frequency calculations were performed in gaseous state using LanL2DZ basis set for the copper metal, whereas 6-311G(d,p) was designated for all other atoms.

Materials and Synthesis
Fine chemicals and solvents were received from the supplier of reagent grade and used directly without further purification. Hydrazine hydrate (90%), carbon disulphide, Cu(II) nitrate trihydrate, and potassium hydroxide were procured from Honeywell Fluka TM , while benzyl chloride and 4-chloroacetophenone were acquired from Manchester Salt and Catalysis Ltd. PerkinElmer Spectrum 1000 FT-IR Spectrometer (PerkinElmer Inc., Waltham, MA, USA) was employed to record the infrared absorption in the wavenumber range of 4000-200 cm −1 in solid state. The UV-Vis measurements were accomplished in methanol solvent using TU-1901 (Purkinje General Instrument Co., Ltd., Beijing, China) double-beam spectrophotometer. The CHN analysis was measured using an Elementar Analyzer Varrio EL (Elementar Analysensysteme GmbH, Langenselbold, Germany).

Synthesis of Copper(II) Complex
First, 0.483 g (2 mmol) of Cu(NO 3 ) 2 ·3H 2 O in ethanol (20 mL) solution was added to a hot solution of 1.340 g (4 mmol), benzyl (E)-2-(1-(4-chlorophenyl)ethylidene)-hydrazine-1carbodithioate ligand in 40 mL of ethanol, where the resulting solution was stirred for one hour. Subsequently, the volume was reduced by one-half and cooled in a refrigerator for about 24 h. The brownish precipitate was separated, washed with ethanol, and dried. The required crystals for XRD were obtained by crystallization from chloroform (25 mL) in the presence of a few drops of n-hexane at room temperature for 3 weeks. The deep-brown solid decomposed at 190 • C and its yield was 86%. Anal. Calcd as C 32 , v(Cu-N) 619. UV-Vis: Ligand bands such as π to π* at 238, 290, 318, and 397 nm, and ligand-to-metal charge transfer (LMCT) band at 455 nm.

XRD-Structure
A single crystal was fixed on a glass fiber for measurement, in which all crystallographic data were accomplished on a Bruker-AXS-SMART APEX CCD diffractometer (Bruker GmbH, Berlin, Germany). by means of Mo-Kα radiation (λ = 0.71073 A • ) and the data were gathered at a temp. of 130 ± 2 K using the scanning technique to a maximum of θ = 27.87 • . The structures were resolved by direct technique using SIR-92 and refined by full-matrix least squares [26]. Non-hydrogen bond atoms were refined anisotropically via SHELXL [27]. Hydrogen atoms were positioned geometrically and refined isotropically. Detailed crystal data and refinement of the structure are reported and depicted in Table 1.

Synthesis of Copper(II) Complex
The Cu(II) complex was prepared by combining two equivalents of free ligand, benzyl (E)-2-(1-(4-chlorophenyl)ethylidene)hydrazine-1-carbodithioate, with one equivalent of Cu(NO 3 ) 2 ·3H 2 O in ethanolic solution [28]. The free thione form of the ligand was subjected to tautomerization to a thiol form [29], (1E,1E)-benzyl hydrogen (1-(4chlorophenyl)ethylidene)carbonhydrazonodithioate, in the solution prior to coordination to the copper metal center. Remarkably, the thione form was an additional stable structure in the solid state [30]. Copper(II) complex was isolated as brown powder and recrystallized from chloroform in the presence of trace amounts of hexane, yielding X-ray quality crystals, the bis[(1E,1E)-benzyl(1-(4-chlorophenyl)ethylidene)-carbonhydrazonodithioate]copper(II) in cis conformation, as in Scheme 1. The XRD analysis reflected a bidentate ligand coordinated through N (azomethine) and S (thiol) to the metal center, giving a solely neutral water-soluble complex.
The new copper complex was characterized by elemental analysis, revealing strong agreement with the expected C 32 H 28 Cl 2 CuN 4 S 4 formula. On the other hand, fast atom bombardment mass spectroscopy (FAB-MS) was used to pursue the molecular weight of the desired complex (Figure 1), giving a value of 730.9 m/z which was quite close to the theoretical assessment (731.3 m/z). These analyses support the general molecular formula of the anticipated Cu(II) complex. The new copper complex was characterized by elemental analysis, revealing strong agreement with the expected C32H28Cl2CuN4S4 formula. On the other hand, fast atom bombardment mass spectroscopy (FAB-MS) was used to pursue the molecular weight of the desired complex (Figure 1), giving a value of 730.9 m/z which was quite close to the theoretical assessment (731.3 m/z). These analyses support the general molecular formula of the anticipated Cu(II) complex.

Infrared and Electronic Absorption Spectra
The solid-state FTIR data of the desired complex displayed few sets of absorption bands for the typical functional groups present in the structure (Figure 2a). The experimental absorption bands in the range of 3015-3110 cm −1 were assigned to aromatic CHstretching vibrations, while the stretching mode at 2980 cm −1 were attributed to aliphatic CH vibration. The absence of free NH and SH absorptions in the region of ~3350 and 2600 cm −1 , respectively, indicates the coordination of the free ligand to the copper metal center The new copper complex was characterized by elemental analysis, revealing strong agreement with the expected C32H28Cl2CuN4S4 formula. On the other hand, fast atom bombardment mass spectroscopy (FAB-MS) was used to pursue the molecular weight of the desired complex (Figure 1), giving a value of 730.9 m/z which was quite close to the theoretical assessment (731.3 m/z). These analyses support the general molecular formula of the anticipated Cu(II) complex.

Infrared and Electronic Absorption Spectra
The solid-state FTIR data of the desired complex displayed few sets of absorption bands for the typical functional groups present in the structure (Figure 2a). The experimental absorption bands in the range of 3015-3110 cm −1 were assigned to aromatic CHstretching vibrations, while the stretching mode at 2980 cm −1 were attributed to aliphatic CH vibration. The absence of free NH and SH absorptions in the region of ~3350 and 2600 cm −1 , respectively, indicates the coordination of the free ligand to the copper metal center

Infrared and Electronic Absorption Spectra
The solid-state FTIR data of the desired complex displayed few sets of absorption bands for the typical functional groups present in the structure (Figure 2a). The experimental absorption bands in the range of 3015-3110 cm −1 were assigned to aromatic CH-stretching vibrations, while the stretching mode at 2980 cm −1 were attributed to aliphatic CH vibration. The absence of free NH and SH absorptions in the region of~3350 and 2600 cm −1 , respectively, indicates the coordination of the free ligand to the copper metal center in a deprotonated form. A weak-stretching vibration at 1605 cm −1 was assigned to a conjugated C=N. Further absorption bands included C-C, C=C, C-N, and C-S. On the other hand, the simulated DFT-FTIR (Figure 2b) of the new complex revealed a sophisticated level of agreement with experimental results; the graphical correlation value (R 2 ) was found to be 0.998, as seen in Figure 2c.
in a deprotonated form. A weak-stretching vibration at 1605 cm −1 was assigned to a conjugated C=N. Further absorption bands included C-C, C=C, C-N, and C-S. On the other hand, the simulated DFT-FTIR (Figure 2b) of the new complex revealed a sophisticated level of agreement with experimental results; the graphical correlation value (R 2 ) was found to be 0.998, as seen in Figure 2c. The experimental and time-dependent TD-DFT electronic absorption spectra of the synthesized copper complex was acquired in a spectral range of 200-800 nm. A solution of the complex in methanol displayed two bands in the UV area at λmax = 260 nm and 315 nm (resulting from π-π* electron transfer) and a single band at λmax = 360 nm, which could be attributed to the n-π* electron transfer. Furthermore, a broad band possessing λmax = 515 nm verified in the visible area can be ascribed to the ligand-to-metal charge transfer as seen in Figure 3a. The simulated electronic spectrum was accomplished using a TD-SCF/DFT/CAM-B3LYP method and 6-31G as basis set in methanol ( Figure 3b) [31,32]. A wide band appeared at λmax = 330 nm with three electron transition lines at 262 nm, 330 nm, and 375 nm, almost covering the three experimental absorptions. A very broad band was estimated at λmax = 560 nm with Δλ = 45 nm of bathochromic shift compared to the same experimental band. The experimental and time-dependent TD-DFT electronic absorption spectra of the synthesized copper complex was acquired in a spectral range of 200-800 nm. A solution of the complex in methanol displayed two bands in the UV area at λ max = 260 nm and 315 nm (resulting from π-π* electron transfer) and a single band at λ max = 360 nm, which could be attributed to the n-π* electron transfer. Furthermore, a broad band possessing λ max = 515 nm verified in the visible area can be ascribed to the ligand-to-metal charge transfer as seen in Figure 3a. The simulated electronic spectrum was accomplished using a TD-SCF/DFT/CAM-B3LYP method and 6-31G as basis set in methanol (Figure 3b) [31,32]. A wide band appeared at λ max = 330 nm with three electron transition lines at 262 nm, 330 nm, and 375 nm, almost covering the three experimental absorptions. A very broad band was estimated at λ max = 560 nm with ∆λ = 45 nm of bathochromic shift compared to the same experimental band.

XRD and DFT
The ORTEP-and DFT-optimized structure diagrams of the cis-Cu(II) complex together with selected structural parameters are illustrated in Figure4 and Table 2. The crystal structure of C32H28Cl2CuN4S4 is a triclinic system with P-1 space group. The full crystallographic data of the desired complex have been reported [33]. The two ligands coor-

XRD and DFT
The ORTEP-and DFT-optimized structure diagrams of the cis-Cu(II) complex together with selected structural parameters are illustrated in Figure 4 and Table 2. The crystal structure of C 32 H 28 Cl 2 CuN 4 S 4 is a triclinic system with P-1 space group. The full crystallographic data of the desired complex have been reported [33]. The two ligands coordinated to the Cu(II) metal center via N,S provided by two anionic Sand two unsaturated N groups to form the neutral bis[(1E,1E)-benzyl(1-(4-chlorophenyl)ethylidene)carbonhydrazonodithioate]copper(II) complex in cis isomer with two metal five-membered Cu(S,N) 2 rings (Figure 4b). It should be noted as well that the trans isomer was not detected at all.
The angles and bond lengths of the desired complex were in a good agreement with similar structures reported previously [9][10][11][12][13][14][15][16][17][18][19][20]. The geometry around the Cu(II) center featured a tetrahedrally distorted square planar with a torsional angle, τ (N1-N3-S3-S1) = 40.7 • (Figure 4b). Based on the DFT optimization of the anticipated complex, the free ligand was coordinated in a deprotonated form, reflecting a neutral structure (Figure 4c,d) with slightly less distortion around (τ = 37.5 • ) around the Cu(II) complex. The level of distortion in DFT calculations were anticipated as geometry optimization performed in a gaseous phase with the absence of intermolecular forces. However, the experimental XRD was performed in solid state in the presence of several types of molecular interactions in the complex lattice. Thus, we highly expected the geometry to be a tetrahedrally distorted square planar, or in other words, the geometry around the copper center could be superiorly described as a square-planar arrangement, exhibiting a tenuous tetrahedral distortion. The DFT calculation additionally showed that the cis-Cu(II) isomer is a stable isomer, since this conformation is kinetically favored and its global energy of formation is less than the thermodynamically favored isomer, trans-form [34].  The DFT-optimized bond lengths and angles were set in a relation with the values resulting from the experimental XRD ( Figure 5). A high level of consistency between the values of DFT and XRD in terms of bond lengths were observed (Figure 5a) with graphical correlation R 2 = 0.995 (Figure 5b). However, bond angles obtained from these two approaches were clearly not in a very good harmonization, in which R 2 = 0.987 (Figure 5c,d). This difference in angle values is due to the difference in the level of distortion around the Cu(II) center, optimized by DFT and measured by XRD. The DFT-optimized bond lengths and angles were set in a relation with the values resulting from the experimental XRD ( Figure 5). A high level of consistency between the values of DFT and XRD in terms of bond lengths were observed (Figure 5a) with graphical correlation R 2 = 0.995 (Figure 5b). However, bond angles obtained from these two approaches were clearly not in a very good harmonization, in which R 2 = 0.987 (Figure 5c,d).  The DFT-optimized bond lengths and angles were set in a relation with the values resulting from the experimental XRD ( Figure 5). A high level of consistency between the values of DFT and XRD in terms of bond lengths were observed (Figure 5a) with graphical correlation R 2 = 0.995 (Figure 5b). However, bond angles obtained from these two approaches were clearly not in a very good harmonization, in which R 2 = 0.987 (Figure 5c,d). This difference in angle values is due to the difference in the level of distortion around the Cu(II) center, optimized by DFT and measured by XRD.

XRD Packing, HSA, and Molecular Electrostatic Potential (MEP) Investigation
Five types of short contacts were detected in the lattice of the cis-Cu(II) complex; all interactions are packed together with cell axes as illustrated in Figure 6a. No classical hydrogen bonding could be found; the shorter hydrogen bond of the type C Ph -H· · · Cl with 2.842 Å reflected a one-dimensional supramolecular chain formation (Figure 6b). However, an R(38) motif was constructed by two C ph -H· · · πPh with a value of 2.860 Å (Figure 6c) and an R(8) motif was detected via -CH· · · πC=N with 2.811 Å (Figure 6d). Two different classical CH· · · π bonds were stabilized by the same phenyl ring via C ph -H· · · πPh with 2.828 Å (Figure 6e), another interaction was categorized as a classical C ph -H· · · πPh with 2.884 Å (Figure 6f), and the last type of interaction was π . . . . π stack interaction in C3-C8 with 3.72 Å bond length as seen in Figure 6g. To gain more information about molecules interacting together in the lattices of cis-Cu(II) complex, HSA and 2D-FP were performed employing the crystallographic information file (CIF) data through CrystalExplorer software [35][36][37][38][39][40]. The simulated results are demonstrated in Figure 7 with declarations of the dnorm, shape index, and 2D-FP established in the range of −0.672 to 1.776 a.u. The presence of heteroatoms and aromatic rings with free lone/pi pair of electrons like S, Cl, and Ph in addition to polar hydrogens in the backbone of the computed complex enhances the formation of many short contacts (Figure 7a). Generally, the surface structure of the cis-Cu(II) complex reflected the existence of ten red spots. The large red spot reflects the consistence of H⸱⸱⸱Cl (H-bond) and CH⸱⸱⸱πC=N interactions, whereas the small spots are due to the formation of Cph-H⸱⸱⸱πPh interactions. The shape index indicates the presence of both nucleophilic (shown in red) Figure 6. Total interaction in the lattice of cis-Cu(II) complex: One-dimensional supramolecular chain formation (a), R(38) motif (b), R(8) motif (c), classical CH· · · π bond short contacts (d), classical C ph -H· · · πPh short contacts (e), and antiparallel π· · · π stack interaction (f).
To gain more information about molecules interacting together in the lattices of cis-Cu(II) complex, HSA and 2D-FP were performed employing the crystallographic information file (CIF) data through CrystalExplorer software [35][36][37][38][39][40]. The simulated results are demonstrated in Figure 7 with declarations of the d norm , shape index, and 2D-FP established in the range of −0.672 to 1.776 a.u. The presence of heteroatoms and aromatic rings with free lone/pi pair of electrons like S, Cl, and Ph in addition to polar hydro-gens in the backbone of the computed complex enhances the formation of many short contacts (Figure 7a). Generally, the surface structure of the cis-Cu(II) complex reflected the existence of ten red spots. The large red spot reflects the consistence of H· · · Cl (Hbond) and CH· · · πC=N interactions, whereas the small spots are due to the formation of C ph -H· · · πPh interactions. The shape index indicates the presence of both nucleophilic (shown in red) and electrophilic (shown in blue) functional groups on the surface of the molecule (Figure 7b). This supports the formation of C-H· · · π Ph interactions as revealed by XRD results. Moreover, the atom-to-atom 2D-FP intermolecular contacts percentage plot reveals the H· · · H interaction with the largest percentage of contribution, while the H· · · Cu demonstrates the smallest percentage of contribution of 0.1% (Figure 7c). The total 2D-FP of H· · · atoms ratios analysis are illustrated as follows: H· · · H > C· · · H > S· · · H > Cl· · · H > N· · · H > Cu· · · H. Moreover, the atom-to-atom 2D-FP intermolecular contacts percentage plot reveals the H⸱⸱⸱H interaction with the largest percentage of contribution, while the H⸱⸱⸱Cu demonstrates the smallest percentage of contribution of 0.1% (Figure 7c). The total 2D-FP of H⸱⸱⸱atoms ratios analysis are illustrated as follows: H⸱⸱⸱H > C⸱⸱⸱H > S⸱⸱⸱H > Cl⸱⸱⸱H > N⸱⸱⸱H > Cu⸱⸱⸱H. The MEP of the complex provided electrophilic and/or nucleophilic data about the surface. For instance, the position and strength of H-bond interactions can be estimated depending on the color around the functional groups, which reflect the electronic density [28][29][30][31][32][33]. The analyzed complex showed a potential decrease in the following order: blue > cyan > green > yellow > orange > red. The MEP also reflected the Cl, N, and S atoms with the highest nucleophilic sites (red color). Meanwhile, Ph rings are labeled with yellow, indicating moderate nucleophilic sites, whereas the green color reflects the neutral functional groups. The electrophilic sites are localized to the protons of phenyl and alkene, as exemplified in Figure 8. Therefore, non-classical C-H⸱⸱⸱π and C-H⸱⸱⸱Cl interactions are observed, revealing a consistence with HSA and XRD outcomes. The MEP of the complex provided electrophilic and/or nucleophilic data about the surface. For instance, the position and strength of H-bond interactions can be estimated depending on the color around the functional groups, which reflect the electronic density [28][29][30][31][32][33]. The analyzed complex showed a potential decrease in the following order: blue > cyan > green > yellow > orange > red. The MEP also reflected the Cl, N, and S atoms with the highest nucleophilic sites (red color). Meanwhile, Ph rings are labeled with yellow, indicating moderate nucleophilic sites, whereas the green color reflects the neutral functional groups. The electrophilic sites are localized to the protons of phenyl and alkene, as exemplified in Figure 8. Therefore, non-classical C-H· · · π and C-H· · · Cl interactions are observed, revealing a consistence with HSA and XRD outcomes.

Thermogravimetric Analysis
In order to demonstrate the thermal stability and material purity of the new metal complex, thermal gravimetric analysis (TGA) of the cis-Cu(II) compound was studied in an open atmosphere with a heat rate of 5 °C/min (Figure 9a).  Figure 9 shows a high thermal stability of the complex, up to ~300 °C. Since no mass loss was detected between 50 and 180 °C, the absence of coordinated or uncoordinated water molecules at the copper metal center supports the XRD result. The mass of the com-

Thermogravimetric Analysis
In order to demonstrate the thermal stability and material purity of the new metal complex, thermal gravimetric analysis (TGA) of the cis-Cu(II) compound was studied in an open atmosphere with a heat rate of 5 • C/min (Figure 9a).

Thermogravimetric Analysis
In order to demonstrate the thermal stability and material purity of the new metal complex, thermal gravimetric analysis (TGA) of the cis-Cu(II) compound was studied in an open atmosphere with a heat rate of 5 °C/min (Figure 9a).  Figure 9 shows a high thermal stability of the complex, up to ~300 °C. Since no mass loss was detected between 50 and 180 °C, the absence of coordinated or uncoordinated water molecules at the copper metal center supports the XRD result. The mass of the com-  Figure 9 shows a high thermal stability of the complex, up to~300 • C. Since no mass loss was detected between 50 and 180 • C, the absence of coordinated or uncoordinated water molecules at the copper metal center supports the XRD result. The mass of the complex was observed to decay in a broad exothermic pattern, starting from 250 • C until completion at 500 • C with DTA = 380 • C. The complex decomposed in one successive broad exothermic step as a simple thermal pattern. In this step, 80% of the mass was lost, while the entire organic moiety was de-structured from the metal center at~500 • C, letting 20% of CuO as a residue, which has been confirmed by FTIR as a broad absorption, ν CuO = 440-520 cm −1 (as seen in Figure 9b). Furthermore, the CuO demonstrated stability between 500 and 800 • C. Above 800 • C the metal oxide lost its O atom to produce pure Cu with an exothermic step at DTA = 810 and 18% of pure Cu metal residue (equation 1). The FTIR of the final residue (Figure 9c) displayed, as expected, the absence of absorption due to the lack of functional groups.

Conclusions
A new copper (II) complex was synthesized with high yield bearing two bidentate N,S-type ligand (benzyl (E)-2-(1-(4-chlorophenyl)ethylidene)hydrazine-1-carbodithioate). The molecular formula was emphasized via UV-Vis, CHN-EA, FT-IR, and FAB-MS analyses. X-ray diffraction revealed that the geometry of the complex is described as a tetrahedrally distorted square planar, in which the two N,S ligands are arranged in cis conformation. Additionally, the HSA and MEP results support the XRD packing in the formation of C-H· · · Cl and C-H· · · π bonds with synthons and supramolecular interactions. The DFT/XRD bond length values are consistent, while a slightly lesser deviation is noted for angles. The thermal stability of the cis-Cu(II) complex is demonstrated to decompose to CuO above 300 • C in a single-step reaction mechanism.